| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184649440-184649756 | Common:4; Rare:102 | ||||
| chr5:218140-218343 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443197 | Common:3; Rare:55 | ||||
| chr5:1801358-1801379 | Rare:6 | ||||
| chr5:6633005-6633369 | Common:8; Rare:115; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:34915502-34915737 | Common:1; Rare:51 | ||||
| chr5:53109750-53109885 | Common:1; Rare:60; Clinvar:1 | ||||
| chr5:60945038-60945146 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr5:61162377-61162477 | Rare:20 | ||||
| chr5:64768621-64768949 | Common:4; Rare:85 | ||||
| chr5:65563132-65563308 | Common:2; Rare:61 | ||||
| chr5:69369488-69369818 | Common:1; Rare:134 | ||||
| chr5:73498365-73498460 | Common:1; Rare:24 | ||||
| chr5:74767117-74767351 | Common:2; Rare:74 | ||||
| chr5:79235980-79236132 | Common:1; Rare:61 |